Alpha thalassemia, but not βS-globin haplotypes, influence sickle cell anemia clinical outcome in a large, single-center Brazilian cohort
Author:
Funder
Conselho Nacional de Desenvolvimento Científico e Tecnológico
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s00277-021-04450-x.pdf
Reference101 articles.
1. Ballas SK, Kesen MR, Goldberg MF, Lutty GA, Dampier C, Osunkwo I, Wang WC, Hoppe C, Hagar W, Darbari DS, Malik P (2012) Beyond the definitions of the phenotypic complications of sickle cell disease: an update on management. Sci World J 2012:1–55. https://doi.org/10.1100/2012/949535
2. Driss A, Asare K, Hibbert J et al (2009) Sickle cell disease in the post genomic era: a monogenic disease with a polygenic phenotype. Genomics Insights 2009:23–48
3. Serjeant GR (2013) The natural history of sickle cell disease. Cold Spring Harb Perspect Med 3:1–11. https://doi.org/10.1101/cshperspect.a011783
4. Kutlar A (2007) Sickle cell disease: a multigenic perspective of a single gene disorder. Hemoglobin 31:209–224. https://doi.org/10.1080/03630260701290233
5. Steinberg MH, Embury SH (1986) Alpha-thalassemia in blacks: genetic and clinical aspects and interactions with the sickle hemoglobin gene. Blood 68:985–990
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